Kinase Inhibitor for Cancer Therapy

Cancer is one of the leading causes of death worldwide, yet considerable efforts are still required to make this pathology curable. Despite the limits of available approaches, kinase inhibitors have marked a turning point in the treatment of different types of tumors. This class of compounds is the...

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Jazyk:angličtina
Vydáno: MDPI - Multidisciplinary Digital Publishing Institute 2024
Témata:
JAK
Src
ALK
UPR
MCL
CML
CMV
TTP
Ras
JNK
n/a
On-line přístup:ONIX_20240704_9783725812905_147
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_version_ 1869520632903892992
collection Directory of Open Access Books
description Cancer is one of the leading causes of death worldwide, yet considerable efforts are still required to make this pathology curable. Despite the limits of available approaches, kinase inhibitors have marked a turning point in the treatment of different types of tumors. This class of compounds is the first oral targeted therapy approved for neoplasia, and about 30 compounds have entered the market in the last five years. Kinase inhibitors include small molecules and monoclonal antibodies and are endowed with fewer side effects than classical antitumor agents. The potential for application of this class of drugs is substantial, and this Special Issue focuses on the discovery and development of kinase inhibitors in terms of in silico studies, synthesis and identification of new compounds, drug delivery, formulation studies, and biological and pharmacokinetic evaluation.
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publisherStr MDPI - Multidisciplinary Digital Publishing Institute
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spelling doab-20.500.12854ir-1393512024-07-04T09:45:20Z Kinase Inhibitor for Cancer Therapy Musumeci, Francesca JAK synthesis kinase inhibitory activity pharmacological uses binding mode/interactions choline kinase lipid metabolism cisplatin lung tumors combinatorial chemotherapy glioblastoma Src pyrazolo [3,4-d]pyrimidine scaffold EGFR multiple myeloma tyrosine kinase treatment ibrutinib gastric cancer kinase inhibitor ALK targeted therapy JNK3 fragment saturation transfer difference NMR X-ray crystallography breast cancer nanomedicine PI3K? poloxamers polymeric nanoparticles TPGS zanubrutinib anthracycline drug resistance aldo-keto reductase 1C3 ABC drug efflux transporter Hsp90 inhibitor co-chaperone heterocycle molecules anticancer agents heat shock proteins ER stress PERK UPR kinase inhibitor cancer diabetes small molecule structure–activity-relationship (SAR) MCL ROR1 small molecules apoptosis AKT1 kinase inhibitors acute myeloid leukemia rare disease molecular modeling molecular docking similarity search MD simulation computer-aided drug discovery cutaneous T-cell lymphoma TWIST1 erufosine curcumin synergy nanotechnology 3D tissue culture 3D tumor model tumor spheroids drug screening preclinical study tyrosine kinase inhibitors innate immunity thyroid cancer tumor-associated macrophages cytokines c-Src/Abl dual inhibitors pyrazolo[3,4-d]pyrimidines ADME antiproliferative activity childhood cancer kinases chemical inhibitors clinical trials dasatinib CML HIV-1 CMV HIV functional cure memory-like NK cells ?? T cells anti-aging senolytic NSCLC KAN0441571C erlotinib TTP rigosertib ON-01910.Na cancer therapy kinase allosteric inhibition Plk1 Ras JNK PI3K/Akt microtubule-destabilizing agents stress-signaling pathways aptamer MNK1 therapeutic target non-small cell lung cancer antitumor 4,5,6,7-tetrabromo-N,N-dimethyl-1H-benzimidazol-2-amine (DMAT) derivatives protein kinase CK2 protein kinase PIM-1 dual protein kinase inhibitors antitumor activity autophagy hepatocellular carcinoma EGFR/PI3K/AKT/mTOR signaling animal models n/a thema EDItEUR::P Mathematics and Science thema EDItEUR::P Mathematics and Science::PS Biology, life sciences thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSD Molecular biology Cancer is one of the leading causes of death worldwide, yet considerable efforts are still required to make this pathology curable. Despite the limits of available approaches, kinase inhibitors have marked a turning point in the treatment of different types of tumors. This class of compounds is the first oral targeted therapy approved for neoplasia, and about 30 compounds have entered the market in the last five years. Kinase inhibitors include small molecules and monoclonal antibodies and are endowed with fewer side effects than classical antitumor agents. The potential for application of this class of drugs is substantial, and this Special Issue focuses on the discovery and development of kinase inhibitors in terms of in silico studies, synthesis and identification of new compounds, drug delivery, formulation studies, and biological and pharmacokinetic evaluation. 2024-07-04T09:45:17Z 2024-07-04T09:45:17Z 2024 book ONIX_20240704_9783725812905_147 9783725812905 9783725812899 https://directory.doabooks.org/handle/20.500.12854/139351 eng application/octet-stream Attribution-NonCommercial-NoDerivatives 4.0 International https://mdpi.com/books/pdfview/book/9349 https://mdpi.com/books/pdfview/book/9349 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-7258-1289-9 10.3390/books978-3-7258-1289-9 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783725812905 9783725812899 518 open access
spellingShingle JAK
synthesis
kinase inhibitory activity
pharmacological uses
binding mode/interactions
choline kinase
lipid metabolism
cisplatin
lung tumors
combinatorial chemotherapy
glioblastoma
Src
pyrazolo [3,4-d]pyrimidine scaffold
EGFR
multiple myeloma
tyrosine kinase
treatment
ibrutinib
gastric cancer
kinase inhibitor
ALK
targeted therapy
JNK3
fragment
saturation transfer difference NMR
X-ray crystallography
breast cancer
nanomedicine
PI3K?
poloxamers
polymeric nanoparticles
TPGS
zanubrutinib
anthracycline
drug resistance
aldo-keto reductase 1C3
ABC drug efflux transporter
Hsp90 inhibitor
co-chaperone
heterocycle molecules
anticancer agents
heat shock proteins
ER stress
PERK
UPR
kinase
inhibitor
cancer
diabetes
small molecule
structure–activity-relationship (SAR)
MCL
ROR1
small molecules
apoptosis
AKT1
kinase inhibitors
acute myeloid leukemia
rare disease
molecular modeling
molecular docking
similarity search
MD simulation
computer-aided drug discovery
cutaneous T-cell lymphoma
TWIST1
erufosine
curcumin
synergy
nanotechnology
3D tissue culture
3D tumor model
tumor spheroids
drug screening
preclinical study
tyrosine kinase inhibitors
innate immunity
thyroid cancer
tumor-associated macrophages
cytokines
c-Src/Abl dual inhibitors
pyrazolo[3,4-d]pyrimidines
ADME
antiproliferative activity
childhood cancer
kinases
chemical inhibitors
clinical trials
dasatinib
CML
HIV-1
CMV
HIV functional cure
memory-like NK cells
?? T cells
anti-aging
senolytic
NSCLC
KAN0441571C
erlotinib
TTP
rigosertib
ON-01910.Na
cancer therapy
kinase allosteric inhibition
Plk1
Ras
JNK
PI3K/Akt
microtubule-destabilizing agents
stress-signaling pathways
aptamer
MNK1
therapeutic target
non-small cell lung cancer
antitumor
4,5,6,7-tetrabromo-N,N-dimethyl-1H-benzimidazol-2-amine (DMAT) derivatives
protein kinase CK2
protein kinase PIM-1
dual protein kinase inhibitors
antitumor activity
autophagy
hepatocellular carcinoma
EGFR/PI3K/AKT/mTOR signaling
animal models
n/a
thema EDItEUR::P Mathematics and Science
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSD Molecular biology
Kinase Inhibitor for Cancer Therapy
title Kinase Inhibitor for Cancer Therapy
title_full Kinase Inhibitor for Cancer Therapy
title_fullStr Kinase Inhibitor for Cancer Therapy
title_full_unstemmed Kinase Inhibitor for Cancer Therapy
title_short Kinase Inhibitor for Cancer Therapy
title_sort kinase inhibitor for cancer therapy
topic JAK
synthesis
kinase inhibitory activity
pharmacological uses
binding mode/interactions
choline kinase
lipid metabolism
cisplatin
lung tumors
combinatorial chemotherapy
glioblastoma
Src
pyrazolo [3,4-d]pyrimidine scaffold
EGFR
multiple myeloma
tyrosine kinase
treatment
ibrutinib
gastric cancer
kinase inhibitor
ALK
targeted therapy
JNK3
fragment
saturation transfer difference NMR
X-ray crystallography
breast cancer
nanomedicine
PI3K?
poloxamers
polymeric nanoparticles
TPGS
zanubrutinib
anthracycline
drug resistance
aldo-keto reductase 1C3
ABC drug efflux transporter
Hsp90 inhibitor
co-chaperone
heterocycle molecules
anticancer agents
heat shock proteins
ER stress
PERK
UPR
kinase
inhibitor
cancer
diabetes
small molecule
structure–activity-relationship (SAR)
MCL
ROR1
small molecules
apoptosis
AKT1
kinase inhibitors
acute myeloid leukemia
rare disease
molecular modeling
molecular docking
similarity search
MD simulation
computer-aided drug discovery
cutaneous T-cell lymphoma
TWIST1
erufosine
curcumin
synergy
nanotechnology
3D tissue culture
3D tumor model
tumor spheroids
drug screening
preclinical study
tyrosine kinase inhibitors
innate immunity
thyroid cancer
tumor-associated macrophages
cytokines
c-Src/Abl dual inhibitors
pyrazolo[3,4-d]pyrimidines
ADME
antiproliferative activity
childhood cancer
kinases
chemical inhibitors
clinical trials
dasatinib
CML
HIV-1
CMV
HIV functional cure
memory-like NK cells
?? T cells
anti-aging
senolytic
NSCLC
KAN0441571C
erlotinib
TTP
rigosertib
ON-01910.Na
cancer therapy
kinase allosteric inhibition
Plk1
Ras
JNK
PI3K/Akt
microtubule-destabilizing agents
stress-signaling pathways
aptamer
MNK1
therapeutic target
non-small cell lung cancer
antitumor
4,5,6,7-tetrabromo-N,N-dimethyl-1H-benzimidazol-2-amine (DMAT) derivatives
protein kinase CK2
protein kinase PIM-1
dual protein kinase inhibitors
antitumor activity
autophagy
hepatocellular carcinoma
EGFR/PI3K/AKT/mTOR signaling
animal models
n/a
thema EDItEUR::P Mathematics and Science
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSD Molecular biology
topic_facet JAK
synthesis
kinase inhibitory activity
pharmacological uses
binding mode/interactions
choline kinase
lipid metabolism
cisplatin
lung tumors
combinatorial chemotherapy
glioblastoma
Src
pyrazolo [3,4-d]pyrimidine scaffold
EGFR
multiple myeloma
tyrosine kinase
treatment
ibrutinib
gastric cancer
kinase inhibitor
ALK
targeted therapy
JNK3
fragment
saturation transfer difference NMR
X-ray crystallography
breast cancer
nanomedicine
PI3K?
poloxamers
polymeric nanoparticles
TPGS
zanubrutinib
anthracycline
drug resistance
aldo-keto reductase 1C3
ABC drug efflux transporter
Hsp90 inhibitor
co-chaperone
heterocycle molecules
anticancer agents
heat shock proteins
ER stress
PERK
UPR
kinase
inhibitor
cancer
diabetes
small molecule
structure–activity-relationship (SAR)
MCL
ROR1
small molecules
apoptosis
AKT1
kinase inhibitors
acute myeloid leukemia
rare disease
molecular modeling
molecular docking
similarity search
MD simulation
computer-aided drug discovery
cutaneous T-cell lymphoma
TWIST1
erufosine
curcumin
synergy
nanotechnology
3D tissue culture
3D tumor model
tumor spheroids
drug screening
preclinical study
tyrosine kinase inhibitors
innate immunity
thyroid cancer
tumor-associated macrophages
cytokines
c-Src/Abl dual inhibitors
pyrazolo[3,4-d]pyrimidines
ADME
antiproliferative activity
childhood cancer
kinases
chemical inhibitors
clinical trials
dasatinib
CML
HIV-1
CMV
HIV functional cure
memory-like NK cells
?? T cells
anti-aging
senolytic
NSCLC
KAN0441571C
erlotinib
TTP
rigosertib
ON-01910.Na
cancer therapy
kinase allosteric inhibition
Plk1
Ras
JNK
PI3K/Akt
microtubule-destabilizing agents
stress-signaling pathways
aptamer
MNK1
therapeutic target
non-small cell lung cancer
antitumor
4,5,6,7-tetrabromo-N,N-dimethyl-1H-benzimidazol-2-amine (DMAT) derivatives
protein kinase CK2
protein kinase PIM-1
dual protein kinase inhibitors
antitumor activity
autophagy
hepatocellular carcinoma
EGFR/PI3K/AKT/mTOR signaling
animal models
n/a
thema EDItEUR::P Mathematics and Science
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSD Molecular biology
url ONIX_20240704_9783725812905_147